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The Journal of Experimental Medicine|September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutationsYi Wang, Cindy S Ma, Yun Ling, et al.
The Journal of Experimental Medicine|June 17, 2021
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominanceTakaki Asano, Joëlle Khourieh, Peng Zhang, et al.
Science (New York, N.Y.)|August 2, 2008
Pyogenic bacterial infections in humans with MyD88 deficiencyHorst von Bernuth, Capucine Picard, Zhongbo Jin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2021
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial diseaseTom Le Voyer, Anna-Lena Neehus, Rui Yang, et al.
Cell Reports|May 14, 2020
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin LesionsMarta Martin-Fernandez, María Bravo García-Morato, Conor Gruber, et al.
The Journal of Experimental Medicine|September 26, 2007
Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunityCheng-Lung Ku, Horst von Bernuth, Capucine Picard, et al.
The Journal of Experimental Medicine|September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiencyJuan Li, Wei-Te Lei, Peng Zhang, et al.
The Journal of Experimental Medicine|November 3, 2022
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosisMasato Ogishi, Rui Yang, Rémy Rodriguez, et al.
The Journal of Experimental Medicine|July 2, 2008
Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cellsLudovic de Beaucoudrey, Anne Puel, Orchidée Filipe-Santos, et al.
The Journal of Experimental Medicine|February 5, 2021
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccinePaul Bastard, Eleftherios Michailidis, Hans-Heinrich Hoffmann, et al.
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